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RAZEK EQUIPAMENTOS LTDA

US

Last updated May 23, 2026

What RAZEK EQUIPAMENTOS LTDA makes

The company produces single-use orthopaedic burs designed for surgical procedures, as well as reusable orthopaedic surgical procedure kits that do not contain medications. These tools are intended for use in orthopaedic surgeries where precision cutting or preparation of bone is required.

The portfolio consists of Class I devices, which are generally considered to pose the lowest risk and are subject to minimal regulatory oversight. These devices are listed in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and compliance with U.S. regulatory requirements. The manufacturer is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Razek Equipamentos Ltda manufacture?

Razek Equipamentos Ltda produces two primary types of orthopaedic devices: single-use orthopaedic burs, which are designed for precise cutting or bone preparation during surgery, and reusable orthopaedic surgical procedure kits that do not contain medications. These tools are specifically intended for orthopaedic procedures where controlled bone manipulation is required.

Where is Razek Equipamentos Ltda based?

Razek Equipamentos Ltda is based in the United States. The company’s location influences its regulatory compliance, particularly in relation to U.S. requirements for device classification and traceability.

How are Razek Equipamentos Ltda’s devices classified under U.S. regulations?

Razek Equipamentos Ltda’s devices fall under Class I classification, which is the lowest risk category for medical devices in the U.S. This classification applies to products like single-use burs and reusable orthopaedic kits that pose minimal risk to patients. Class I devices typically require less regulatory scrutiny, though they must still meet basic safety and performance standards.

Are Razek Equipamentos Ltda’s devices listed in any regulatory databases?

Yes, Razek Equipamentos Ltda’s devices are included in the FDA’s Unique Device Identifier (UDI) database. The UDI system ensures traceability and compliance by assigning a unique identifier to each device, helping track its distribution, usage, and regulatory status. This is particularly important for Class I devices, which must still adhere to labeling and manufacturing requirements.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
—
FDA FEI Number
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DUNS Number
898213154

Catalogue (11827)

Page 220 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 732781900
FDA UDI
Class IActive
Razek Equipamentos 736100100
FDA UDI
Class IActive
Razek Equipamentos 738690350
FDA UDI
Class IActive
Razek Equipamentos 738650260
FDA UDI
Class IActive
Razek Equipamentos 738430040
FDA UDI
Class IActive
Razek Equipamentos 738711940
FDA UDI
Class IActive
Razek Equipamentos 738731690
FDA UDI
Class IActive
Razek Equipamentos 733222000
FDA UDI
Class IActive
Razek Equipamentos 736940000
FDA UDI
Class IActive
Razek Equipamentos 733322100
FDA UDI
Class IActive
Razek Equipamentos 978610000
FDA UDI
Class IActive
Razek Equipamentos 738410110
FDA UDI
Class IActive
Razek Equipamentos 738670100
FDA UDI
Class IActive
Razek Equipamentos 738360300
FDA UDI
Class IActive
Razek Equipamentos 738740630
FDA UDI
Class IActive
Razek Equipamentos 738711220
FDA UDI
Class IActive
Razek Equipamentos 740250002
FDA UDI
Class IActive
Razek Equipamentos 490061190
FDA UDI
Class IActive
Razek Equipamentos 974970000
FDA UDI
Class IActive
Razek Equipamentos 978850870
FDA UDI
Class IActive
Razek Equipamentos 733361100
FDA UDI
Class IActive
Razek Equipamentos 979010330
FDA UDI
Class IActive
Razek Equipamentos 978881080
FDA UDI
Class IActive
Razek Equipamentos 736590500
FDA UDI
Class IActive
Razek Equipamentos 738440500
FDA UDI
Class IActive
Razek Equipamentos 738640090
FDA UDI
Class IActive
Razek Equipamentos 930360810
FDA UDI
Class IActive
Razek Equipamentos 978823200
FDA UDI
Class IActive
Razek Equipamentos 734740000
FDA UDI
Class IActive
Razek Equipamentos 732841300
FDA UDI
Class IActive
Razek Equipamentos 978851070
FDA UDI
Class IActive
Razek Equipamentos 978421300
FDA UDI
Class IActive
Razek Equipamentos 736280300
FDA UDI
Class IActive
Razek Equipamentos 738270000
FDA UDI
Class IActive
Razek Equipamentos 734360100
FDA UDI
Class IActive
Razek Equipamentos 730280010
FDA UDI
Class IActive
Razek Equipamentos 738670210
FDA UDI
Class IActive
Razek Equipamentos 738420270
FDA UDI
Class IActive
Razek Equipamentos 738390540
FDA UDI
Class IActive
Razek Equipamentos 738730190
FDA UDI
Class IActive
Razek Equipamentos 738210090
FDA UDI
Class IActive
Razek Equipamentos 733360800
FDA UDI
Class IActive
Razek Equipamentos 738390720
FDA UDI
Class IActive
Razek Equipamentos 738360910
FDA UDI
Class IActive
Razek Equipamentos 979081260
FDA UDI
Class IActive
Razek Equipamentos 978870740
FDA UDI
Class IActive
Razek Equipamentos 978560600
FDA UDI
Class IActive
Razek Equipamentos 978511800
FDA UDI
Class IActive
Razek Equipamentos 738430370
FDA UDI
Class IActive
Razek Equipamentos 490060830
FDA UDI
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

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Authorities

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Razek Equipamentos Ltda Sao Carlos Sao Paulo · BR FEI 3021907852